Canonical Allele Identifier: CA022822
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 17901
ClinVar RCV Id: RCV001837442 RCV001851950
dbSNP Id: rs121918391
MyVariant Identifiers: chr2:g.21238041A>T (hg19) chr2:g.21015169A>T (hg38)
PubMed: PMID:15984016
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015169A>T , CM000664.2:g.21015169A>T GRCh38
NC_000002.11:g.21238041A>T , CM000664.1:g.21238041A>T GRCh37
NC_000002.10:g.21091546A>T NCBI36
NG_011793.1:g.33905T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*2906T>A ENSP00000501110.2:n.*2906T>A
ENST00000673882.2:c.*2695T>A ENSP00000501253.2:n.*2695T>A
ENST00000673739.1:c.3314T>A ENSP00000501110.1:n.3314T>A
ENST00000673882.1:c.3103T>A ENSP00000501253.1:n.3103T>A
ENST00000233242.5:c.3600T>A MANE Select ENSP00000233242.1:p.Tyr1200Ter
ENST00000616098.4:c.3600T>A ENSP00000477990.1:p.Tyr1200Ter
NM_000384.2:c.3600T>A NP_000375.2:p.Tyr1200Ter
XM_011532809.1:c.3600T>A XP_011531111.1:p.Tyr1200Ter
NM_000384.3:c.3600T>A MANE Select NP_000375.3:p.Tyr1200Ter
Search 100 bp 5'
Search 100 bp 3'